ch-22 HW answers - HCC Learning Web
... C) organic bases that react with acids to form ammonium salts. D) organic acids that react with bases to form ammonium salts. E) None of the above. ...
... C) organic bases that react with acids to form ammonium salts. D) organic acids that react with bases to form ammonium salts. E) None of the above. ...
alcohols - GCG-42
... • Based on the no. of hydroxyl groups the alcohols are classified as mono-, di- and trihydric accordingly, if the molecules contain 1, 2 or 3 –OH groups respectively. The alcohols which contain four or more no. of –OH groups are called polyhydric alcohols. ...
... • Based on the no. of hydroxyl groups the alcohols are classified as mono-, di- and trihydric accordingly, if the molecules contain 1, 2 or 3 –OH groups respectively. The alcohols which contain four or more no. of –OH groups are called polyhydric alcohols. ...
Reactions of esters:
... But enzyme is required for this hydrolysis reaction in body. The body has no enzymes inside cells that can catalyze this reaction. So energy rich diphosphates can exist in cells despite the abundance of water. Adenosine triphosphate, or ATP, is the most common and widely occurring member of a small ...
... But enzyme is required for this hydrolysis reaction in body. The body has no enzymes inside cells that can catalyze this reaction. So energy rich diphosphates can exist in cells despite the abundance of water. Adenosine triphosphate, or ATP, is the most common and widely occurring member of a small ...
Functional Groups
... functional group: an atom, or group of atoms (with specific connectivity), exhibiting identical chemical reactivity regardless of the molecule containing it; the reactivity of individual functional groups dictates the reactivity of the molecule of which they are a part ...
... functional group: an atom, or group of atoms (with specific connectivity), exhibiting identical chemical reactivity regardless of the molecule containing it; the reactivity of individual functional groups dictates the reactivity of the molecule of which they are a part ...
chm 103 general chemistry
... H. Organics Containing Oxygen 1. Alcohols: Organics containing –O—H (hydroxyl) groups a. Methanol (methyl alcohol): CH3OH Imagine methane (CH4) with one H replaced by OH (but it is not made this way) Generally manufactured from synthesis gas (CO + H2) under conditions of high temperature and pre ...
... H. Organics Containing Oxygen 1. Alcohols: Organics containing –O—H (hydroxyl) groups a. Methanol (methyl alcohol): CH3OH Imagine methane (CH4) with one H replaced by OH (but it is not made this way) Generally manufactured from synthesis gas (CO + H2) under conditions of high temperature and pre ...
Part B: Short Written Response - bourre-chem-11
... 3. Please explain why are alkenes more reactive than alkanes, in spite of the fact that double bonds are “stronger” than single bonds? (1 mark) ...
... 3. Please explain why are alkenes more reactive than alkanes, in spite of the fact that double bonds are “stronger” than single bonds? (1 mark) ...
Salame - The City College of New York
... The CCNY policy on academic integrity will be followed in this course. The document can be found through the CCNY website by clicking on Current Students Academic Services Policy on Academic Integrity. All students must read the details regarding plagiarism and cheating in order to be familiar w ...
... The CCNY policy on academic integrity will be followed in this course. The document can be found through the CCNY website by clicking on Current Students Academic Services Policy on Academic Integrity. All students must read the details regarding plagiarism and cheating in order to be familiar w ...
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... (d)Wurtz's reaction 9. Primary alcohols can be obtained from the reaction of the RMgX (a) CO 2 (b) HCHO (c) CH 3 CHO (d) H 2 O ...
... (d)Wurtz's reaction 9. Primary alcohols can be obtained from the reaction of the RMgX (a) CO 2 (b) HCHO (c) CH 3 CHO (d) H 2 O ...
6.5 Organic Lecture
... – Alkenes are hydrocarbons with at least one double carbon to carbon bond. • To show the presence of the double bond, the –ane suffix from the alkane name is changed to –ene. – The alkenes are unsaturated with respect to hydrogen • This means it does not have the maximum number of hydrogen atoms as ...
... – Alkenes are hydrocarbons with at least one double carbon to carbon bond. • To show the presence of the double bond, the –ane suffix from the alkane name is changed to –ene. – The alkenes are unsaturated with respect to hydrogen • This means it does not have the maximum number of hydrogen atoms as ...
10.3 Alcohols
... the carbon attached to the -OH group. • Number the carbons in this chain so that the carbon attached to the -OH group has the lowest number. • Drop the -e ending from the name of the parent alkane and replace it with –ol • Alcohols containing two or three -OH groups are called diols and triols. ...
... the carbon attached to the -OH group. • Number the carbons in this chain so that the carbon attached to the -OH group has the lowest number. • Drop the -e ending from the name of the parent alkane and replace it with –ol • Alcohols containing two or three -OH groups are called diols and triols. ...
Alkanes Chapter 1.1
... in a molecule is replaced by another atom or group of atoms • Alkanes react in a specific type of substitution reaction called halogenation where a hydrogen atom is replaced by a halogen atom (Cl, Br, etc.) to form an alkyl halide catalyst ...
... in a molecule is replaced by another atom or group of atoms • Alkanes react in a specific type of substitution reaction called halogenation where a hydrogen atom is replaced by a halogen atom (Cl, Br, etc.) to form an alkyl halide catalyst ...
Chemistry activity 10 organic structures
... How organic molecules react depends on the functional groups they contain. Very often during a reaction the carbon backbone of a molecule remains unchanged and the action takes place at the heteroatoms – that is, the atoms other than carbon and hydrogen. The most common heteroatoms in organic molecu ...
... How organic molecules react depends on the functional groups they contain. Very often during a reaction the carbon backbone of a molecule remains unchanged and the action takes place at the heteroatoms – that is, the atoms other than carbon and hydrogen. The most common heteroatoms in organic molecu ...
IB Chemistry HL Assessment Statements 2009 Revised
... Include the identification of the repeating unit. ...
... Include the identification of the repeating unit. ...
CHAPTER 11 BONDING AND MOLECULAR STRUCTURE:
... • Reducing aldehydes and acids with NaBH4 or LiAlH4 produces a primary alcohol. • Reduction of a ketone produces a secondary alcohol. ...
... • Reducing aldehydes and acids with NaBH4 or LiAlH4 produces a primary alcohol. • Reduction of a ketone produces a secondary alcohol. ...
Week 11 Problem Set (Solutions)
... into Br’s via an SN2-type mechanism, so an inversion of configuration must have occurred. EtO- is a strong unhindered base that will perform an E2 elimination towards the more substituted side. Interestingly, we see that the alkene formed is not the most substituted alkene possible. This leaves us w ...
... into Br’s via an SN2-type mechanism, so an inversion of configuration must have occurred. EtO- is a strong unhindered base that will perform an E2 elimination towards the more substituted side. Interestingly, we see that the alkene formed is not the most substituted alkene possible. This leaves us w ...
The Chemicals of Life Properties of Organic Compounds • Organic
... It has a high electronegativity, so it pulls electrons away from the carbon atom It is important in carbohydrates, pyruvic acid (used in respiration), glycerol (a component of fats), and alcohols Alcohols are compounds that contain a hydroxyl group (OH-) attached to the carbon, and can easily ...
... It has a high electronegativity, so it pulls electrons away from the carbon atom It is important in carbohydrates, pyruvic acid (used in respiration), glycerol (a component of fats), and alcohols Alcohols are compounds that contain a hydroxyl group (OH-) attached to the carbon, and can easily ...
Alcohols/Wade
... 5. What carbonyl compound and reducing agent would you use to carry out the reduction to form the following alcohols? a) n-octanol ...
... 5. What carbonyl compound and reducing agent would you use to carry out the reduction to form the following alcohols? a) n-octanol ...
PREPARATION OF ORGANOLITHIUM COMPOUNDS - GCG-42
... Since oxygen is more electronegative than carbon, the carbonyl group is electron-deficient at carbon, that is, it is an electrophile. The organometallic compound (R-Li) behaves as a nucleophile with an unshared pair on the carbon. ...
... Since oxygen is more electronegative than carbon, the carbonyl group is electron-deficient at carbon, that is, it is an electrophile. The organometallic compound (R-Li) behaves as a nucleophile with an unshared pair on the carbon. ...
Organic Chemistry
... Carbon forms 4 bonds (C has 4 valence e-) Nitrogen forms 3 bonds (N has 5 valence e-) Oxygen forms 2 bonds (O has 6 valence e-) Hydrogen forms 1 bond (H breaks the octet rule) Halogens form 1 bond (all have 7 valence e-) ...
... Carbon forms 4 bonds (C has 4 valence e-) Nitrogen forms 3 bonds (N has 5 valence e-) Oxygen forms 2 bonds (O has 6 valence e-) Hydrogen forms 1 bond (H breaks the octet rule) Halogens form 1 bond (all have 7 valence e-) ...
conversion of the OH group into a better leaving group, and
... • For an alcohol to undergo nucleophilic substitution, OH must be converted into a better leaving group. By using acid, ¯OH can be converted into H2O, a good leaving group. ...
... • For an alcohol to undergo nucleophilic substitution, OH must be converted into a better leaving group. By using acid, ¯OH can be converted into H2O, a good leaving group. ...
Chem 3.5 #6 Amines
... Write an equation which shows a reaction that could be used to produce CH3CH2NH2 from CH3CH2Cl. ...
... Write an equation which shows a reaction that could be used to produce CH3CH2NH2 from CH3CH2Cl. ...
Organic Compounds
... These temporary dipoles hold alkanes as liquids or solids, and must be overcome in order to vaporize a liquid or melt a solid (wax) ...
... These temporary dipoles hold alkanes as liquids or solids, and must be overcome in order to vaporize a liquid or melt a solid (wax) ...
SCH4U Unit Test Name
... a. the smallest aldehyde has the formula HCOH b. a carbonyl carbon consists of a carbon-oxygen double bond c. in an aldehyde, the carbonyl carbon is always bonded to a hydrogen atom d. Ketones are more soluble in water than alcohols with the equivalent number of carbons ____ 17. The correct name for ...
... a. the smallest aldehyde has the formula HCOH b. a carbonyl carbon consists of a carbon-oxygen double bond c. in an aldehyde, the carbonyl carbon is always bonded to a hydrogen atom d. Ketones are more soluble in water than alcohols with the equivalent number of carbons ____ 17. The correct name for ...
Haloalkane
The haloalkanes (also known, as halogenoalkanes or alkyl halides) are a group of chemical compounds derived from alkanes containing one or more halogens. They are a subset of the general class of halocarbons, although the distinction is not often made. Haloalkanes are widely used commercially and, consequently, are known under many chemical and commercial names. They are used as flame retardants, fire extinguishants, refrigerants, propellants, solvents, and pharmaceuticals. Subsequent to the widespread use in commerce, many halocarbons have also been shown to be serious pollutants and toxins. For example, the chlorofluorocarbons have been shown to lead to ozone depletion. Methyl bromide is a controversial fumigant. Only haloalkanes which contain chlorine, bromine, and iodine are a threat to the ozone layer, but fluorinated volatile haloalkanes in theory may have activity as greenhouse gases. Methyl iodide, a naturally occurring substance, however, does not have ozone-depleting properties and the United States Environmental Protection Agency has designated the compound a non-ozone layer depleter. For more information, see Halomethane. Haloalkane or alkyl halides are the compounds which have the general formula ″RX″ where R is an alkyl or substituted alkyl group and X is a halogen (F, Cl, Br, I).Haloalkanes have been known for centuries. Chloroethane was produced synthetically in the 15th century. The systematic synthesis of such compounds developed in the 19th century in step with the development of organic chemistry and the understanding of the structure of alkanes. Methods were developed for the selective formation of C-halogen bonds. Especially versatile methods included the addition of halogens to alkenes, hydrohalogenation of alkenes, and the conversion of alcohols to alkyl halides. These methods are so reliable and so easily implemented that haloalkanes became cheaply available for use in industrial chemistry because the halide could be further replaced by other functional groups.While most haloalkanes are human-produced, non-artificial-source haloalkanes do occur on Earth, mostly through enzyme-mediated synthesis by bacteria, fungi, and especially sea macroalgae (seaweeds). More than 1600 halogenated organics have been identified, with bromoalkanes being the most common haloalkanes. Brominated organics in biology range from biologically produced methyl bromide to non-alkane aromatics and unsaturates (indoles, terpenes, acetogenins, and phenols). Halogenated alkanes in land plants are more rare, but do occur, as for example the fluoroacetate produced as a toxin by at least 40 species of known plants. Specific dehalogenase enzymes in bacteria which remove halogens from haloalkanes, are also known.